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遗传性球形红细胞增多症在小儿溶血性贫血中并非罕见,我院从1961年至1978年收治13例。13例中,最早于生后3天发病,最迟者至生后11年多发病。全部病例有不同程度的皮肤、粘膜苍白,发热,黄疸,肝脾肿大,其肿大程度与病程长短无关,其中1例伴有胆石症。实验室资料:红细胞一般在100～300万/立方毫米,血红蛋白在4～8克%。血片中9例可见较多球形红细胞。5例作红细胞平均直径(MCD)
Hereditary spherocytosis in children with hemolytic anemia is not uncommon, our hospital from 1961 to 1978, 13 cases were admitted. 13 cases, the earliest onset in 3 days after birth, the latest to more than 11 years after birth incidence. All cases have different degrees of skin, mucous membrane pale, fever, jaundice, hepatosplenomegaly, and its extent has nothing to do with the duration of the disease, of which 1 case associated with cholelithiasis. Laboratory information: red blood cells generally in the 100 to 3 million / cubic mm, hemoglobin in 4 to 8 grams%. Blood film in 9 cases showed more spherical red blood cells. 5 cases of red blood cell mean diameter (MCD)